EP0434145A2 - Acrylamid Copolymere die Benzol-dicarbonsäure(Meth)acrylamideinheiten enthalten - Google Patents

Acrylamid Copolymere die Benzol-dicarbonsäure(Meth)acrylamideinheiten enthalten Download PDF

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Publication number
EP0434145A2
EP0434145A2 EP90203318A EP90203318A EP0434145A2 EP 0434145 A2 EP0434145 A2 EP 0434145A2 EP 90203318 A EP90203318 A EP 90203318A EP 90203318 A EP90203318 A EP 90203318A EP 0434145 A2 EP0434145 A2 EP 0434145A2
Authority
EP
European Patent Office
Prior art keywords
acrylamide
units
benzene dicarboxylic
copolymers according
copolymers
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP90203318A
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English (en)
French (fr)
Other versions
EP0434145A3 (en
EP0434145B1 (de
Inventor
Fabrizio Bonaccorsi
Rosario Pappa
Umberto Cova
Arnaldo Roggero
Thomas Paul Lockhart
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eni Tecnologie SpA
Original Assignee
Agip SpA
Eniricerche SpA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agip SpA, Eniricerche SpA filed Critical Agip SpA
Publication of EP0434145A2 publication Critical patent/EP0434145A2/de
Publication of EP0434145A3 publication Critical patent/EP0434145A3/en
Application granted granted Critical
Publication of EP0434145B1 publication Critical patent/EP0434145B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/53—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/55—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a carbon atom of an unsaturated carbon skeleton

Definitions

  • This invention concerns new acrylamide copolymers consisting of (meta)acrylamide benzene dicarboxylic monomer units as in the following formula: wherein R is H or CH3; X is H or alcaline metal, preferably sodium or potassium, or NH4; and wherein the COOX groups may be in ortho-, meta- or para- position in relation to each other, preferably being in ortho-position to each other; and of (met) acrylamide monomer (II) units, the molar ratio between units (I) and units (II) varying between 1:99 and 99:1.
  • Homopolymers and copolymers with acrylamides containing benzene (met) acrylamide units with the benzene ring carrying a carboxylic and an hydroxylic unit in ortho- position to each other, are known in the art.
  • Such polymers can form complexes with metals, for instance titanium, and as described in US patent 3 794 563, these complexes may be used as solid supports for fixed enzymes.
  • the copolymers are used preferably with a molar ratio between formula (I) monomer units and formula (II) monomer units which varies between 70:30 and 99:1.
  • Copolymers in this invention may also be used with flocculants to precipitate solids suspended in water.
  • they are preferably used with a molar ratio of (I):(II) between 1:99 and 30:70.
  • Copolymers in this invention are also water-soluble in very high concentrations and have a weight average molecular weight which goes from 1000 to 20,000,000 and preferably from 1,000,000 to 10,000,000.
  • Normal practice features an aqueous solution, with a pH going from 3 to 11 approximately, using radical initiators, for instance peroxides, persulphates or nitrogen compounds.
  • radical initiators for instance peroxides, persulphates or nitrogen compounds.
  • the copolymerisation reaction temperature may generally vary between ambient temperature (15°-25°C) and 90°C approximately and conversion of the monomers is practically complete within a period going from 30 minutes to 24 hours depending on the temperature used, the usual procedure generally featuring a temperature of 50°-70°C for a period of 1-2 hours.
  • the molar ratio of the monomers thus introduced is also maintained unchanged in the final copolymer.
  • Formula (III) (met)acrylamide benzene dicarboxylic monomers used in the production of copolymers according to the present invention may be obtained quite simply according to known organic chemistry methodology.
  • preparation may start with commercially available relevant nitro benzene dicarboxylic compounds, by reducing the nitro group to an amino group, for instance using the hydrogenation process on platinum oxide described in the Journal of Organic Chemistry 25 , 1882 (1960), followed by condensation of the amino benzene dicarboxylic compound with (met)acryloyl chloride.
  • the following examples are given for illustration purposes only and must not be considered as in any way restrictive of the scope of the invention.
  • the mixture is left for 2 hours under nitrogen flow to remove any air contained therein, then heated to 60°C and a solution of 85,5 mg (0.316 mmoles) of K2S2O8 in 5 ml of de-ionised water is added quickly. The reaction is allowed to continue for 90 minutes, maintaining the temperature at 60°C.
  • the molar ratio between 3-acrylamide-1,2-benzene dicarboxylic and acrylamide units is 3:97.
  • the copolymer properties are as follows: Weight average molecular weight: 3,700,000 (g/mole); (determined by GPC) Intrinsic viscosity (determined in aqueous solution of 2M NaCl at 25°C): 950 cm3/g.
  • the conversion rate is 95% and the ratio between monomer units of the copolymer, assessed by 13C-NMR spectroscopic analysis, is practically equal to the initial rate (4.9 : 95.1).
  • copolymer properties are as follows: Weight average molecular weight: 8,200,000 g/mole Intrinsic viscosity: 1585 cm3/g
  • the copolymer properties are as follows: The conversion rate is 97% and the ratio between monomer units is practically equal to the initial rate (4.7 : 95.3).
  • the properties of the copolymer thus obtained are as follows: Weight average molecular weight: 4,400,000 g/mole Intrinsic viscosity: 1050 cm3/g
  • the ratio between monomer units in the copolymer is 4.5 : 95.5.
  • the properties of the copolymer thus obtained are as follows: Weight average molecular weight: 3,915,000 g/mole Intrinsic viscosity: 890 cm3/g.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP90203318A 1989-12-21 1990-12-13 Acrylamid Copolymere die Benzol-dicarbonsäure(Meth)acrylamideinheiten enthalten Expired - Lifetime EP0434145B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT02280089A IT1237794B (it) 1989-12-21 1989-12-21 Copolimeri acrilammidici contenenti unita' (met) acrilammido benzendicarbossiliche
IT2280089 1989-12-21

Publications (3)

Publication Number Publication Date
EP0434145A2 true EP0434145A2 (de) 1991-06-26
EP0434145A3 EP0434145A3 (en) 1991-10-16
EP0434145B1 EP0434145B1 (de) 1998-08-12

Family

ID=11200573

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90203318A Expired - Lifetime EP0434145B1 (de) 1989-12-21 1990-12-13 Acrylamid Copolymere die Benzol-dicarbonsäure(Meth)acrylamideinheiten enthalten

Country Status (9)

Country Link
US (1) US5103057A (de)
EP (1) EP0434145B1 (de)
JP (1) JPH04126708A (de)
BR (1) BR9006503A (de)
CA (1) CA2032758C (de)
DK (1) DK0434145T3 (de)
ES (1) ES2120945T3 (de)
IT (1) IT1237794B (de)
NO (1) NO176107C (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5219476A (en) * 1989-03-31 1993-06-15 Eniricerche S.P.A. Gellable aqueous composition and its use in enhanced petroleum recovery

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1249256B (de) * 1967-09-07 Farbenfabriken Bayer Aktiengesellschaft, Leverkusen Verfahren zur Herstellung ungesättigter polymerisierbarer Carbonsäureamide
FR2012370A1 (fr) * 1968-07-05 1970-03-20 Basf Ag Procede pour la preparation de nappes azurees optiquement
US3598792A (en) * 1969-11-19 1971-08-10 Grace W R & Co Polymers from diesters of n-acrylyliminodiacetic acids
JPS57105409A (en) * 1980-12-20 1982-06-30 Lion Corp Bonding composition for dental use
EP0487153A1 (de) * 1990-11-23 1992-05-27 ENIRICERCHE S.p.A. Gelierbare wässrige Zusammensetzungen, welche Polymere mit speziellen chelatierenden funktionellen Gruppen enthalten, verwendbar für die Ölgewinnung in Ölfeldern

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1352739A (en) * 1971-09-01 1974-05-08 Aspro Nicholas Ltd Polymer-enzyme complexes
US4237253A (en) * 1977-04-21 1980-12-02 L'oreal Copolymers, their process of preparation, and cosmetic compounds containing them
US4668747A (en) * 1984-09-24 1987-05-26 Allied Corporation Preparation of water soluble cationic acrylamide polymer and product using weak acid to adjust pH

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1249256B (de) * 1967-09-07 Farbenfabriken Bayer Aktiengesellschaft, Leverkusen Verfahren zur Herstellung ungesättigter polymerisierbarer Carbonsäureamide
FR2012370A1 (fr) * 1968-07-05 1970-03-20 Basf Ag Procede pour la preparation de nappes azurees optiquement
US3598792A (en) * 1969-11-19 1971-08-10 Grace W R & Co Polymers from diesters of n-acrylyliminodiacetic acids
JPS57105409A (en) * 1980-12-20 1982-06-30 Lion Corp Bonding composition for dental use
EP0487153A1 (de) * 1990-11-23 1992-05-27 ENIRICERCHE S.p.A. Gelierbare wässrige Zusammensetzungen, welche Polymere mit speziellen chelatierenden funktionellen Gruppen enthalten, verwendbar für die Ölgewinnung in Ölfeldern

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE CHEMICAL ABSTRACTS, (HOST:STN), no. 82(16), abstract no. 98923u, American Chemical Society, US; B.P. NIKOL'SKII et al.: "Synthesis and physicochemical properties of a cation exchanger containing phthalate functional groups", & ZH. OBSHCH. KHIM., 44(11), 2558-61 1974 *
PATENT ABSTRACTS OF JAPAN, vol. 6, no. 191 (C-127)[1069], 30th September 1982; & JP-A-57 105 409 (RAION K.K.) 30-06-1982 *

Also Published As

Publication number Publication date
DK0434145T3 (da) 1999-05-10
IT8922800A0 (it) 1989-12-21
EP0434145A3 (en) 1991-10-16
NO176107C (no) 1995-02-01
EP0434145B1 (de) 1998-08-12
CA2032758A1 (en) 1991-06-22
NO905451D0 (no) 1990-12-18
CA2032758C (en) 2002-06-18
BR9006503A (pt) 1991-10-01
JPH04126708A (ja) 1992-04-27
NO176107B (no) 1994-10-24
NO905451L (no) 1991-06-24
IT1237794B (it) 1993-06-17
US5103057A (en) 1992-04-07
ES2120945T3 (es) 1998-11-16

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